{{Rsnum
|rsid=62514891
|Chromosome=12
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=PAH
|position=102917130
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PAH
}}{{omim
|id=612349
|rsnum=62514891
|variant=0009
}}{{ClinVar
|rsid=62514891
|Reversed=1
|FwdREF=A
|FwdALT=G,T
|REF=T
|ALT=A,C
|RSPOS=103310908
|CHROM=12
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050360000000000002110100
|GENEINFO=PAH:5053
|GENE_NAME=PAH
|GENE_ID=5053
|WGT=0
|VC=SNV
|CLNALLE=2
|CLNHGVS=NC_000012.11:g.103310908T>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=612349.0009
|CLNCUI=.,C0031485; C0751435
|CLNDBN=Phenylketonuria; Hyperphenylalaninemia, non-pku
|Disease=Phenylketonuria; Hyperphenylalaninemia
|CLNACC=RCV000000616.2; RCV000000617.2
|Tags=RV;PM;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT; MedGen
|CLNDSDBID=NBK1504:C0031485:261600:2209:716:154735006; C0751435
|CLNSIG=5
}}